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BioWorld - Wednesday, December 31, 2025
Home » Topics » Infection » Coronavirus

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Disintegrating coronavirus

CSL, University of Queensland quit COVID-19 vaccine trials due to HIV antibody response

Dec. 11, 2020
By Tamra Sami
PERTH, Australia – The University of Queensland (UQ) and CSL Ltd. are abandoning their trials of an Australian COVID-19 vaccine after recipients generated HIV antibodies during phase I trials. The response means the antibodies produced by the vaccine can interfere with HIV diagnostic tests. However, there was no possibility the vaccine caused infection, and routine follow-up tests confirmed no HIV virus was present, the partners said.
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Regulatory actions for Dec. 11, 2020

Dec. 11, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Arix, Biogen, Bristol Myers Squibb, Daiichi Sankyo, Dynavax Technologies, Excellthera, Gilead Sciences, Janssen, Lexicon, Merck, Passage, Sanofi, Seagen, Soleno, V2act, Viiv Healthcare, Xeris.
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Other news to note for Dec. 11, 2020

Dec. 11, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Active, Astrazeneca, Bristol Myers, Cipla, Fera, Immunitybio, Immunoprecise, Innate, Medivir, Neotx, Pear, Polyphor, Quralis, Tetralogic.
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In the clinic for Dec. 11, 2020

Dec. 11, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Akari, Geron, Greenwich Lifesciences, Mitsubishi Tanabe, Prevail, Puma, Puretech Health, Scyneis, Sellas Life Sciences, Tychan.
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Vaccine administration

Vaccine EUA not a total slam dunk with adcom

Dec. 10, 2020
By Mari Serebrov
The FDA’s vaccine advisory committee voted 17-4 with one abstention Dec. 10 to recommend an emergency use authorization (EUA) for the Pfizer Inc./Biontech SE mRNA vaccine BNT-162b2 to prevent COVID-19 in individuals 16 and older.
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Elecsys Anti-SARS-COV-2 packaging

Roche teams up with Moderna for vaccine trials

Dec. 10, 2020
By Liz Hollis
Roche Holding AG has revealed a partnership with Moderna Inc. involving the use of the Elecsys Anti-SARS-CoV-2 S antibody test in the latter’s mRNA-1273 vaccine research trials. The news comes shortly after Roche received emergency use authorization from the U.S. FDA for the antibody test. 
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Pixel by LabCorp

Labcorp snags EUA for first direct-to-consumer COVID-19 test

Dec. 10, 2020
By Meg Bryant
The U.S. FDA has made it easier for people who want to get tested for COVID-19, granting emergency use authorization (EUA) for direct-to-consumer sales of Laboratory Corp. of America Holdings’ (Labcorp) Pixel COVID-19 test home collection kit. With this latest EUA, any individual 18 years and older can purchase the Pixel test system without a prescription.
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BioWorld MedTech’s Diagnostics Extra for Dec. 10, 2020

Dec. 10, 2020
By Meg Bryant and Anette Breindl
Keeping you up to date on recent developments in diagnostics, including: Predicting breast cancer recurrence, Comparing SARS-CoV-2 PCR tests, Paying attention to the little guy in proteomics, Increasing biomarker reproducibility
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Regulatory front

House passes stopgap spending bill

Dec. 10, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Senate passes counterfeit device destruction bill; MHRA posts device compliance dates for Brexit.
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Regulatory actions for Dec. 10, 2020

Dec. 10, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Advanced Bionics, Advanced Medtech, Laboratory Corporation of America, Oxford Immunotec Global, Recor Medical, Virocule.
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